Scientists map rare brain disorder to pave way for First-Ever cures
NCT ID NCT06625112
Summary
This study aims to prepare for future clinical trials for STXBP1-related disorders, a rare and severe genetic condition causing seizures and developmental delays. Researchers will follow 120 patients over time to better understand how the disease progresses and to identify the best ways to measure if future treatments work. The goal is to gather the essential information needed to design effective trials for potential new therapies.
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Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
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Contact
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Locations
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Universitair Ziekenhuis Antwerpen
RECRUITINGAntwerp, Belgium
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Conditions
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